Canonical Allele Identifier: CA2575085700

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611651_13611654del , CM000674.2:g.13611651_13611654del	GRCh38
NC_000012.11:g.13764585_13764588del , CM000674.1:g.13764585_13764588del	GRCh37
NC_000012.10:g.13655852_13655855del	NCBI36
NG_031854.1:g.373437_373440del
NG_031854.2:g.375361_375364del

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1780+73_1780+76del MANE Select	ENSP00000477455.1:n.1780+73_1780+76del
ENST00000609686.3:c.1780+73_1780+76del	ENSP00000477455.1:n.1780+73_1780+76del
NM_000834.3:c.1780+73_1780+76del	NP_000825.2:n.1780+73_1780+76del
XM_011520628.1:c.1780+73_1780+76del	XP_011518930.1:n.1780+73_1780+76del
XM_011520629.1:c.1780+73_1780+76del	XP_011518931.1:n.1780+73_1780+76del
XM_011520630.1:c.1780+73_1780+76del	XP_011518932.1:n.1780+73_1780+76del
XR_931372.1:n.179-3447_179-3444del
XR_931373.1:n.318+2894_318+2897del
XR_931374.1:n.117+1051_117+1054del
NM_000834.4:c.1780+73_1780+76del	NP_000825.2:n.1780+73_1780+76del
XM_011520628.2:c.1780+73_1780+76del	XP_011518930.1:n.1780+73_1780+76del
XM_011520629.2:c.1780+73_1780+76del	XP_011518931.1:n.1780+73_1780+76del
XM_017019219.2:c.1780+73_1780+76del	XP_016874708.1:n.1780+73_1780+76del
XR_001749013.1:n.599+1051_599+1054del
XR_931372.2:n.316-3447_316-3444del
XR_931373.2:n.457+2894_457+2897del
NM_000834.5:c.1780+73_1780+76del MANE Select	NP_000825.2:n.1780+73_1780+76del